(1R)-3,3-二甲基双环[2.2.1]庚烷-2-甲酰氯 | 61175-88-0

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 中文名称: (1R)-3,3-二甲基双环[2.2.1]庚烷-2-甲酰氯
• 英文名称: (1R,2R,4S)-3,3-dimethylbicyclo[2.2.1]heptane-2-carbonyl chloride
• CAS: 61175-88-0；67596-91-2；85440-78-4
• 化学式: C₁₀H₁₅ClO
• 分子量: 186.681
• InChiKey: MMJZYLSOVDKRTC-CSMHCCOUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.82
• 重原子数：
  12.0
• 可旋转键数：
  1.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.9
• 拓扑面积：
  17.07
• 氢给体数：
  0.0
• 氢受体数：
  1.0

反应信息

• 作为反应物：
  描述：

  (1R)-3,3-二甲基双环[2.2.1]庚烷-2-甲酰氯 在 水 作用下， 以 1,4-二氧六环 、 乙醚 为溶剂， 反应 21.0h， 生成 endo-3,3-Dimethylbicyclo<2.2.1>heptane-2-acetic acid
  参考文献：
  名称：

  Site-selective rhodium(II) acetate mediated intramolecular metal-carbene insertions into carbon-hydrogen bonds of bicyclo[2.2.1]heptanes: effcient syntheses of (+)-albene and (-)-.beta.-santalene

  摘要：

  Treatment of alpha-diazo ketones 1a-d and 2a-d with catalytic amounts of rhodium(II) acetate led to selective carbene insertions into C-H bonds resulting in cyclopentane-annulated products in high yields. The highly selective insertion realized into the exo-methyl C-H bond of 1a has been utilized in the syntheses of (+)-albene (8) and (-)-beta-santalene (11).

  DOI：

  10.1021/jo00004a019
• 作为产物：
  描述：

  endo-2,2-dimethylbicyclo<2.2.1>heptane-3-carboxylic acid 在 草酰氯 作用下， 以 正己烷 为溶剂， 反应 4.0h， 生成 (1R)-3,3-二甲基双环[2.2.1]庚烷-2-甲酰氯
  参考文献：
  名称：

  Site-selective rhodium(II) acetate mediated intramolecular metal-carbene insertions into carbon-hydrogen bonds of bicyclo[2.2.1]heptanes: effcient syntheses of (+)-albene and (-)-.beta.-santalene

  摘要：

  Treatment of alpha-diazo ketones 1a-d and 2a-d with catalytic amounts of rhodium(II) acetate led to selective carbene insertions into C-H bonds resulting in cyclopentane-annulated products in high yields. The highly selective insertion realized into the exo-methyl C-H bond of 1a has been utilized in the syntheses of (+)-albene (8) and (-)-beta-santalene (11).

  DOI：

  10.1021/jo00004a019

文献信息

• Site-selective rhodium(II) acetate mediated intramolecular metal-carbene insertions into carbon-hydrogen bonds of bicyclo[2.2.1]heptanes: effcient syntheses of (+)-albene and (-)-.beta.-santalene
  作者：Harikisan R. Sonawane、Nanjundiah S. Bellur、Jaimala R. Ahuja、Dilip G. Kulkarni

  DOI：10.1021/jo00004a019

  日期：1991.2

  Treatment of alpha-diazo ketones 1a-d and 2a-d with catalytic amounts of rhodium(II) acetate led to selective carbene insertions into C-H bonds resulting in cyclopentane-annulated products in high yields. The highly selective insertion realized into the exo-methyl C-H bond of 1a has been utilized in the syntheses of (+)-albene (8) and (-)-beta-santalene (11).